Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Should genetic testing for SCAs be included in the diagnostic workup for MSA?

Neurology - 4 Nov 2014

Kim Han-Joon, Jeon Beom S, Shin Junghwan, Lee Woong-Woo, Park Hyeyoung, Jung Yu Jin, Ehm Gwanhee

Abstract excerpt

OBJECTIVE: To examine the prevalence of mutations in spinocerebellar ataxia (SCA) genes in patients who were clinically diagnosed with multiple system atrophy (MSA). METHODS: Genetic tests for SCA were performed in 302 of 528 patients who met the diagnostic criteria for MSA based on clinical features. Generally, when a patient had cerebellar symptoms or cerebellar atrophy on neuroimaging, genetic tests for SCA...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Age of Onset
Share to Aged
Share to Genetic Testing

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Multiple System Atrophy

Share to Mutation

Share to Spinocerebellar Ataxias

Source

Identifiers

PMID: 25298309
DOI: 10.1212/WNL.0000000000000965

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Should genetic testing for SCAs be included in the diagnostic workup for MSA?PMID 25298309Read ↗

Other causes of ataxia in patients with SCA mutations.Semantic proximity Read ↗

Spinocerebellar Ataxia in Brazil: A Comprehensive Genotype - Phenotype Analysis.Semantic proximity Read ↗

Spinocerebellar degenerations.Semantic proximity Read ↗

Spinocerebellar Ataxia in Brazil: A Comprehensive Genotype–Phenotype AnalysisSemantic proximity Read ↗

Spinocerebellar Ataxia Type 23 (SCA23): a rare cause of SCA in the AmericasSemantic proximity Read ↗

Frequency analysis and clinical characterization of spinocerebellar ataxia types 1, 2, 3, 6, and 7 in Korean patients.Semantic proximity Read ↗

Evidence and practices of the use of next generation sequencing in patients with undiagnosed autosomal dominant cerebellar ataxias: a review.Semantic proximity Read ↗

Multiplex families with multiple system atrophy.Semantic proximity Read ↗

Movement disorders in spinocerebellar ataxias in a cohort of Brazilian patients.Semantic proximity Read ↗

Initially with pure parkinsonian phenotype of spinocerebellar ataxia type 3: A rare case report and literature reviewSemantic proximity Read ↗

The clinical diagnosis of autosomal dominant spinocerebellar ataxias.Semantic proximity Read ↗

Fragile X-associated tremor/ataxia syndrome: phenotypic comparisons with other movement disorders.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.